US5098917A - Substituted imidazolylmethyloxiranes and substituted imidazolypropenes their preparation and fungicides containing them - Google Patents
Substituted imidazolylmethyloxiranes and substituted imidazolypropenes their preparation and fungicides containing them Download PDFInfo
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/64—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with substituted hydrocarbon radicals attached to ring carbon atoms, e.g. histidine
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
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- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/68—Halogen atoms
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/70—One oxygen atom
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/90—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/91—Nitro radicals
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/91—Nitro radicals
- C07D233/92—Nitro radicals attached in position 4 or 5
- C07D233/93—Nitro radicals attached in position 4 or 5 with hydrocarbon radicals, substituted by halogen atoms, attached to other ring members
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
Definitions
- the present invention relates to novel substituted imidazolylmethyloxiranes and substituted imidazolylpropenes, processes for their preparation and fungicides containing them, and methods for controlling fungi.
- imidazolyloxiranes for example cis-2-(imidazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2,6-difluorophenyl)-oxirane (DE-32 18 130) can be used as fungicides.
- the fungicidal actions are unsatisfactory.
- R 1 and R 2 are identical or different and are each C 1 14 C 8 -alkyl, C 3 -C 8 -cycloalkyl, C 5 -C 8 -cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, and these radicals may be monosubstituted to trisubstituted by halogen, nitro, phenoxy, amino, alkyl, alkoxy or haloalkyl, each of 1 to 4 carbon atoms, and D is O or a single bond, E is H, F, Cl or Br and X, Y and Z are identical or different and are each hydrogen, halogen, nitro, cyano, C 1 -C 3 -acyl, C 1 -C 3 -haloal
- the compounds of the formula I contain asymmetric carbon atoms and can therefore occur as enantiomers and diastereomers.
- the mixtures of diastereomers can be separated in a conventional manner, for example on the basis of their different solubilities or by column chromatography, and can be isolated in pure form.
- the racemates of the novel compounds can be resolved by known methods, for example by salt formation with an optically active acid, separation of the diastereomeric salts and liberation of the enantiomers by means of a base. Both the pure diastereomers or enantiomers and the mixtures of these obtained in the synthesis can be used as fungicides.
- R 1 and R 2 are each, for example, C 1 -C 8 -alkyl, in particular C 1 -C 4 -alkyl, such as methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, tert-butyl, n-pentyl or neopentyl, 1-naphthyl, 2-naphthyl, p-biphenyl, phenyl, halophenyl, such as 2-chlorophenyl, 2-fluorophenyl, 2-bromophenyl, 3-chlorophenyl, 3-bromophenyl, 3-fluorophenyl, 4-fluorophenyl, 4-chlorophenyl, 4-bromophenyl, 2,4-dichlorophenyl,2,3-dichlorophenyl,2,5-dichlorophenyl, 2,6-dichlorophenyl
- X, Y and Z are each, for example, hydrogen, methyl, ethyl, propyl, isopropyl, trifluoromethyl, methoxy, ethoxy, methylamino, dimethylamino, acetylamino, diacetylamino, methylthio, acetyl, methoxyacetyl, phenyl, halophenyl, chlorophenyl or hydroxyethyl, and X, Y and Z cannot simultaneously be hydrogen, ie. one or more of the radicals X, Y and Z differ from hydrogen.
- Acid addition salts are, for example, the hydrochlorides, bromides, sulfates, nitrates, phosphates, oxalates and dodecylbenzenesulfonates.
- the activity of the salts is attributable to the cation, so that the anion is generally unimportant.
- novel active ingredients salts are prepared by reacting an imidazolylmethyloxirane (I) with an acid.
- Metal complexes of the active ingredients I or their salts can be formed, for example, with copper, zinc, tin, manganese, iron, cobalt or nickel, by reacting the imidazolylmethyloxirane with a corresponding metal salt, for example with copper sulfate, zinc chloride, tin chloride or manganese sulfate.
- reaction a) is carried out, for example, in the presence or absence of a base and in the presence or absence of a solvent or diluent, with or without the addition of a reaction accelerator, at from 10° to 120° C.
- the preferred solvents and diluents include ketones, such as acetone, methyl ethyl ketone and cyclohexanone, nitriles, such as acetonitrile and propionitrile, alcohols, such as methanol, ethanol, isopropanol, n-butanol and glycol, esters, such as ethyl acetate, methyl acetate and butyl acetate, ethers, such as tetrahydrofuran, diethyl ether, dimethoxyethane, dioxane and diisopropyl ether, amides, such as dimethylformamide, dimethylacetamide and N-methylpyrrolidone, and dimethyl s
- Suitable bases which may also be used as acid acceptors in the reaction are, for example, alkali metal hydroxides, such as lithium hydroxide, sodium hydroxide or potassium hydroxide, alkali metal carbonates, such as sodium carbonate, potassium carbonate or cesium carbonate, or sodium bicarbonate, potassium bicarbonate, cesium bicarbonate, pyridine or 4-dimethylaminopyridine.
- alkali metal hydroxides such as lithium hydroxide, sodium hydroxide or potassium hydroxide
- alkali metal carbonates such as sodium carbonate, potassium carbonate or cesium carbonate
- sodium bicarbonate potassium bicarbonate, cesium bicarbonate
- pyridine sodium bicarbonate
- 4-dimethylaminopyridine sodium bicarbonate
- other conventional bases may also be used.
- Preferred reaction accelerators are metal halides, such as sodium iodide or potassium iodide, quaternary ammonium salts, such as tetrabutylammonium chloride, bromide, iodide or bisulfate, benzyltriethylammonium chloride or bromide, and crown ethers, such as 12-crown-4, 15-crown-5, 18-crown-6, dibenzo-18-crown-6 or dicyclohexano-18-crown-6.
- metal halides such as sodium iodide or potassium iodide
- quaternary ammonium salts such as tetrabutylammonium chloride, bromide, iodide or bisulfate, benzyltriethylammonium chloride or bromide
- crown ethers such as 12-crown-4, 15-crown-5, 18-crown-6, dibenzo-18-crown
- the reaction is generally carried out at, for example, from 20° to 150° C., under atmospheric or super atmospheric pressure, continuously or batchwise.
- reaction a) is carried out, for example, in the presence or absence of a solvent or diluent and with or without the addition of a strong inorganic or organic base, at from -10° to 120° C.
- a solvent or diluent include amides, such as dimethylformamide, diethylformamide, dimethylacetamide, diethylacetamide, N-methylpyrrolidone, hexamethylphosphorotriamide, sulfoxides, such as dimethyl sulfoxide, and finally sulfolane.
- Suitable bases which may also be used as acid acceptors in the reaction, are, for example, alkali metal hydrides, such as lithium hydride, sodium hydride and potassium hydride, alkali metal amides, such as sodium amide and potassium amide, as well as sodium tert-butoxide, potassium tert-butoxide, triphenylmethyllithium, triphenylmethylsodium, triphenylmethylpotassium, naphthalenelithium, naphthalenesodium and naphthalenepotassium.
- alkali metal hydrides such as lithium hydride, sodium hydride and potassium hydride
- alkali metal amides such as sodium amide and potassium amide
- sodium tert-butoxide potassium tert-butoxide
- Suitable diluents for reaction b) are polar organic solvents, such as nitriles, eg. acetonitrile, sulfoxides, eg. dimethyl sulfoxide, formamides, eg. dimethylformamide, ketones, eg. acetone, ethers, eg. diethyl ether or tetrahydrofuram, and in particular chlorohydrocarbons, eg. methylene chloride and chloroform.
- polar organic solvents such as nitriles, eg. acetonitrile, sulfoxides, eg. dimethyl sulfoxide, formamides, eg. dimethylformamide, ketones, eg. acetone, ethers, eg. diethyl ether or tetrahydrofuram, and in particular chlorohydrocarbons, eg. methylene chloride and chloroform.
- the reaction is carried out in general at, for example, from 0° to 100° C., preferably from 20° to 80° C. In the presence of a solvent, it is advantageously carried out at the boiling point of the particular solvent.
- novel starting compounds II are obtained, for example, by epoxidation of the corresponding olefins V ##STR6## (cf. G. Dittus in Houben-Weyl-Muller, Methoden der Organischen Chemie, Georg Thieme Verlag, Stuttgart, 1965, Vol. VI, 3, page 385 et seq.).
- the compound V is prepared by halogenating or oxidizing olefins of the formula IX ##STR7## by know methods in the allyl position.
- Suitable halogenating reagents are N-chloro- and N-bromosuccinimide in halohydrocarbons, such as carbon tetrachloride, trichloroethane or methylene chloride, temperatures of from 20° to 100° C. being employed.
- halohydrocarbons such as carbon tetrachloride, trichloroethane or methylene chloride
- temperatures of from 20° to 100° C. being employed.
- peresters such as tert-butyl perbenzoate or tert-butyl peracetate
- a heavy metal salt eg. copper(I) chloride or copper(I) bromide.
- the reaction is carried out in an inert solvent at from 10° to 100° C.
- the olefins V are oxidized with a peroxycarboxylic acid, such as perbenzoic acid, 3-chloroperbenzoic acid, 4-nitroperbenzoic acid, monoperphthalic acid, peracetic acid, perpropionic acid, permaleic acid, monopersuccinic acid, perpelargonic acid or trifluoroperacetic acid, in an inert solvent, preferably a chlorohydrocarbon, eg.
- a buffer such as sodium acetate, sodium carbonate, disodium hydrogen phosphate or Triton B.
- the reaction is carried out at from 10° to 100° C. and, if required, is catalyzed with, for example, iodine, sodium tungstate or light.
- tert-butyl hydroperoxide with the addition of a catalyst, eg. sodium tungstate, pertungstic acid, molybdenum hexacarbonyl or vanadyl acetylacetonate, are also suitable for the oxidation.
- a catalyst eg. sodium tungstate, pertungstic acid, molybdenum hexacarbonyl or vanadyl acetylacetonate.
- the reactive esters which can be reacted with III are prepared by generally known methods (Houben-Weyl-Muller, Methoden der organischen Chemie, Georg Thieme Verlag, Stuttgart, 1955, Volume 9, pages 388, 663 and 671).
- Examples of such esters are methanesulfonates, trifluoromethanesulfonates, 2,2,2-trifluoroethanesulfonates, nonafluorobutanesulfonates, 4-methylbenzenesulfonates, 4-bromobenzenesulfonates, 4-nitrobenzenesulfonates and benzenesulfonates.
- the compounds V can be prepared by generally known processes of olefin synthesis (Houben-Weyl-Muller, Methoden der organischen Chemie, Georg Thieme Verlag, Stuttgart, 1972, Vol. V, 1b).
- the compounds of the formula IV ##STR8## are obtained, for example, by a) reacting a compound of the formula V ##STR9## where R 1 and R 2 have the abovementioned meanings and L is a leaving group which can be substituted by a nucleophile, with a compound of the formula III ##STR10## where Me is hydrogen, a metal atom or trimethylsilyl and X, Y and Z have the above mentioned meanings, or reacting a compound of the formula VI ##STR11## where R 1 , X, Y and Z have the abovementioned meanings, with a compound of the formula VII ##STR12## where R 2 has the same meanings as in formula I and R 3 , R 4 and R 5 may be identical or different and are each phenyl, p-carboxyphenyl, p-dimethylaminophenyl, dimethylamino, piperidino, morpholino, alkyl of 1 to
- the compounds of the formula I in which E is F, Cl or Br can be prepared, for example, by reacting a compound of the formula VIII ##STR13## where R 1 , R 2 and D have the state meanings, with a compound of the formula III ##STR14## where X, Y, Z and Me have the abovementioned meanings, in the presence of a thionyl halide.
- the reaction is carried out, for example, in the presence or absence of a solvent or diluent at from -30° to 80° C.
- a solvent or diluent include nitriles, such as acetonitrile or, propionitrile, ethers, such as tetrahydrofuran, diethyl ether, dimethoxyethane, dioxane or diisopropyl ether, and in particular hydrocarbons and chlorohydrocarbons, such as pentane, hexane, toluene, methylene chloride, chloroform, carbon tetrachloride or dichloroethane, or mixtures of these.
- novel starting compounds VIII in which D is O are obtained, for example, by epoxidation of the corresponding olefins X ##STR15## (cf. G. Dittus in Houben-Weyl-Muller, Methoden der Organischen Chemie, Georg Thieme Verlag, Stuttgart, 1965, Vol. VI, 3, page 38 et seq.).
- the compounds X can be prepared by generally known methods of aldehyde synthesis (Houben-Weyl-Muller, Methoden der Organischen Chemie, Georg Thieme Verlag, Stuttgart, 1983, Vol. E3).
- novel compounds are extremely effective on a broad spectrum of phytopathogenic fungi, in particular those from the Ascomycetes and Basidiomycetes classes. Some of them have a systemic action and can be used as foliar and soil fungicides.
- the fungicidal compounds are of particular interest for controlling a large number of fungi in various crops or their seeds, especially wheat, rye, barley, oats, rice, Indian corn, lawns, cotton, soybeans, coffee, sugar cane, fruit and ornamentals in horticulture and viticulture, and in vegetables such as cucumbers, beans and cucurbits.
- novel compounds are particularly useful for controlling the following plant diseases:
- Botrytis cinerea (gray mold) in strawberries and grapes
- the compounds are applied by spraying or dusting the plants with the active ingredients, or treating the seeds of the plants with the active ingredients. They may be applied before or after infection of the plants or seeds by the fungi.
- novel substances can be converted into conventional formulations such as solutions, emulsions, suspensions, dusts, powders, pastes and granules.
- the application forms depend entirely on the purposes for which they are intended; they should at all events ensure a fine and uniform distribution of the active ingredient.
- the formulations are produced in known manner, for example by extending the active ingredient with solvents and/or carriers, with or without the use of emulsifiers and dispersants; if water is used as solvent, it is also possible to employ other organic solvents as auxiliary solvents.
- auxiliaries for this purpose are solvents such as aromatics (e.g., xylene), chlorinated aromatics (e.g., chlorobenzenes), paraffins (e.g., crude oil fractions), alcohols (e.g., methanol, butanol), ketones (e.g., cyclohexanone), amines (e.g., ethanolamine, dimethylformamide), and water; carriers such as ground natural minerals (e.g., kaolins, aluminas, talc and chalk) and ground synthetic minerals (e.g., highly disperse silica and silicates); emulsifiers such as nonionic and anionic emulsifiers (e.g., polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates); and dispersants such as lignin, sulfite waste liquors and methylcellulose.
- solvents such as aromatics (e.g.,
- the fungicidal agents generally contain from 0.1 to 95, and preferably from 0.5 to 90, wt % of active ingredient.
- the application rates are from 0.02 to 3 kg or more of active ingredient per hectare, depending on the type of effect desired.
- the novel compounds may also be used for protecting materials, for example against Paecilomyces variotii.
- agents and the ready-to-use formulations prepared from them such as solutions, emulsions, suspensions, powders, dusts, pastes and granules, are applied in conventional manner, for example by spraying, atomizing, dusting, scattering, dressing or watering.
- V. 80 parts by weight of compound no. 113 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene- ⁇ -sulfonic acid, 10 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 7 parts by weight of powdered silica gel, and triturated in a hammer mill. By uniformly distributing the mixture in water, a spray liquor is obtained.
- the agents according to the invention may also be present together with other active ingredients, for example herbicides, insecticides, growth regulators, and fungicides, and may furthermore be mixed and applied together with fertilizers. Admixture with other fungicides frequently results in an increase in the fungicidal spectrum.
- fungicides which may be combined with the novel compounds are;
- heterocyclic substances such as
- Leaves of potted vines of the Muller-Thurgau variety were sprayed with aqueous suspensions containing (dry basis) 80% of active ingredient and 20% of emulsifier. To assess the duration of action, the plants were set up, after the sprayed-on layer had dried, for 8 days in the greenhouse. Then the leaves were infected with a zoospore suspension of Plasmopara viticola. The plants were first placed for 48 hours in a water vapor-saturated chamber at 24° C. and then in a greenhouse for 5 days at from 20° to 30° C. To accelerate and intensify the sporangiophore discharge, the plants were then again placed in the moist chamber for 16 hours. The extent of fungus attack was then assessed on the undersides of the leaves.
Abstract
Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes of the general formula I ##STR1## wherein R1 and R2 are alkyl, cycloalkyl, cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl,
D is oxygen or a single bond,
E is H, F, Cl or Br,
X, Y and Z are hydrogen, halogen, nitro, cyano, alkyl, haloalkyl, alkoxy, unsubstituted or substituted amino, unsubstituted or substituted mercapto, acyl, alkoxycarbonyl, hydroxyalkyl or substituted or unsubstituted phenyl, and acid addition salts and metal complexes thereof tolerated by plants,
processes for their manufacture, and fungicides containing them.
Description
This is a division of application Ser. No. 07,377,000, filed on July 7, 1989, now U.S. Pat. No. 5,028618.
The present invention relates to novel substituted imidazolylmethyloxiranes and substituted imidazolylpropenes, processes for their preparation and fungicides containing them, and methods for controlling fungi.
It is known that imidazolyloxiranes, for example cis-2-(imidazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2,6-difluorophenyl)-oxirane (DE-32 18 130) can be used as fungicides. However, the fungicidal actions are unsatisfactory.
We have found that substituted imidazolylmethyloxiranes and substituted imidazolylpropenes of the formula I ##STR2## where R1 and R2 are identical or different and are each C1 14 C8 -alkyl, C3 -C8 -cycloalkyl, C5 -C8 -cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, and these radicals may be monosubstituted to trisubstituted by halogen, nitro, phenoxy, amino, alkyl, alkoxy or haloalkyl, each of 1 to 4 carbon atoms, and D is O or a single bond, E is H, F, Cl or Br and X, Y and Z are identical or different and are each hydrogen, halogen, nitro, cyano, C1 -C3 -acyl, C1 -C3 -haloalkyl, C1 -C3 -alkoxy, amino which is unsubstituted or substituted by C1 -C3 -alkyl or C1 -C3 -acyl, unsubstituted or C1 -C3 -alkyl-substituted mercapto, C1 -C3 -acyl, C1 -C3 -alkoxycarbonyl, C1 -C3 -hydroxyalkyl or unsubstituted or substituted phenyl, and X, Y and Z cannot simultaneously be hydrogen, and their plant-tolerated acid addition salts and metal complexes have a better fungicidal action than known azole compounds.
The compounds of the formula I contain asymmetric carbon atoms and can therefore occur as enantiomers and diastereomers. In the case of the novel compounds, the mixtures of diastereomers can be separated in a conventional manner, for example on the basis of their different solubilities or by column chromatography, and can be isolated in pure form. The racemates of the novel compounds can be resolved by known methods, for example by salt formation with an optically active acid, separation of the diastereomeric salts and liberation of the enantiomers by means of a base. Both the pure diastereomers or enantiomers and the mixtures of these obtained in the synthesis can be used as fungicides.
R1 and R2 are each, for example, C1 -C8 -alkyl, in particular C1 -C4 -alkyl, such as methyl, ethyl, isopropyl, n-propyl, n-butyl, sec-butyl, tert-butyl, n-pentyl or neopentyl, 1-naphthyl, 2-naphthyl, p-biphenyl, phenyl, halophenyl, such as 2-chlorophenyl, 2-fluorophenyl, 2-bromophenyl, 3-chlorophenyl, 3-bromophenyl, 3-fluorophenyl, 4-fluorophenyl, 4-chlorophenyl, 4-bromophenyl, 2,4-dichlorophenyl,2,3-dichlorophenyl,2,5-dichlorophenyl, 2,6-dichlorophenyl, 2-chloro-6-fluorophenyl or 2-chloro-4-fluorophenyl, C1 -C4 -alkoxyphenyl, such as 2-methoxyphenyl, 3-methoxyphenyl, 4-methoxyphenyl, 2,4-dimethoxyphenyl or 3,4-dimethoxyphenyl, C1 -C4 -alkylphenyl, such as 4-ethylphenyl, 4-isopropylphenyl, 4-tert-butylphenyl or 4-tert-butoxyphenyl, 2-chloro-6-methylphenyl, 3-phenoxyphenyl, 4-phenoxyphenyl, 3-nitrophenyl, 4-nitrophenyl, 3-aminophenyl, 4-aminophenyl, 2-aminophenyl, 2-trifluoromethylphenyl, 3-trifluoromethylphenyl, 4-trifluoromethylphenyl, 3-pyridyl, tetrahydropyranyl, cyclopropyl, cyclopentyl, cyclohexyl, 2-cyclohexenyl, 3-cyclohexenyl or norbornyl.
X, Y and Z are each, for example, hydrogen, methyl, ethyl, propyl, isopropyl, trifluoromethyl, methoxy, ethoxy, methylamino, dimethylamino, acetylamino, diacetylamino, methylthio, acetyl, methoxyacetyl, phenyl, halophenyl, chlorophenyl or hydroxyethyl, and X, Y and Z cannot simultaneously be hydrogen, ie. one or more of the radicals X, Y and Z differ from hydrogen.
Acid addition salts are, for example, the hydrochlorides, bromides, sulfates, nitrates, phosphates, oxalates and dodecylbenzenesulfonates. The activity of the salts is attributable to the cation, so that the anion is generally unimportant. The novel active ingredients salts are prepared by reacting an imidazolylmethyloxirane (I) with an acid.
Metal complexes of the active ingredients I or their salts can be formed, for example, with copper, zinc, tin, manganese, iron, cobalt or nickel, by reacting the imidazolylmethyloxirane with a corresponding metal salt, for example with copper sulfate, zinc chloride, tin chloride or manganese sulfate.
The compounds of the formula I in which D is O and E is H can be prepared, for example by
a) reacting a compound of the formula II ##STR3## where R1 and R2 have the abovementioned meanings and L is a leaving group which can be substituted by a nucleophile (eg. halogen or OH), with a compound of the formula III ##STR4## where Me is hydrogen, a metal atom (eg. Na or K) or trimethylsilyl and X, Y and Z have the abovementioned meanings, or
b) converting a compound of the formula IV ##STR5## where R1, R2, X, Y and Z have the abovementioned meanings, into the epoxide.
If Me is hydrogen, reaction a) is carried out, for example, in the presence or absence of a base and in the presence or absence of a solvent or diluent, with or without the addition of a reaction accelerator, at from 10° to 120° C. The preferred solvents and diluents include ketones, such as acetone, methyl ethyl ketone and cyclohexanone, nitriles, such as acetonitrile and propionitrile, alcohols, such as methanol, ethanol, isopropanol, n-butanol and glycol, esters, such as ethyl acetate, methyl acetate and butyl acetate, ethers, such as tetrahydrofuran, diethyl ether, dimethoxyethane, dioxane and diisopropyl ether, amides, such as dimethylformamide, dimethylacetamide and N-methylpyrrolidone, and dimethyl sulfoxide, sulfolane and mixtures of these.
Suitable bases, which may also be used as acid acceptors in the reaction are, for example, alkali metal hydroxides, such as lithium hydroxide, sodium hydroxide or potassium hydroxide, alkali metal carbonates, such as sodium carbonate, potassium carbonate or cesium carbonate, or sodium bicarbonate, potassium bicarbonate, cesium bicarbonate, pyridine or 4-dimethylaminopyridine. However, other conventional bases may also be used.
Preferred reaction accelerators are metal halides, such as sodium iodide or potassium iodide, quaternary ammonium salts, such as tetrabutylammonium chloride, bromide, iodide or bisulfate, benzyltriethylammonium chloride or bromide, and crown ethers, such as 12-crown-4, 15-crown-5, 18-crown-6, dibenzo-18-crown-6 or dicyclohexano-18-crown-6.
The reaction is generally carried out at, for example, from 20° to 150° C., under atmospheric or super atmospheric pressure, continuously or batchwise.
If Me is a metal atom, reaction a) is carried out, for example, in the presence or absence of a solvent or diluent and with or without the addition of a strong inorganic or organic base, at from -10° to 120° C. The preferred solvents and diluents include amides, such as dimethylformamide, diethylformamide, dimethylacetamide, diethylacetamide, N-methylpyrrolidone, hexamethylphosphorotriamide, sulfoxides, such as dimethyl sulfoxide, and finally sulfolane.
Suitable bases, which may also be used as acid acceptors in the reaction, are, for example, alkali metal hydrides, such as lithium hydride, sodium hydride and potassium hydride, alkali metal amides, such as sodium amide and potassium amide, as well as sodium tert-butoxide, potassium tert-butoxide, triphenylmethyllithium, triphenylmethylsodium, triphenylmethylpotassium, naphthalenelithium, naphthalenesodium and naphthalenepotassium.
Examples of suitable diluents for reaction b) are polar organic solvents, such as nitriles, eg. acetonitrile, sulfoxides, eg. dimethyl sulfoxide, formamides, eg. dimethylformamide, ketones, eg. acetone, ethers, eg. diethyl ether or tetrahydrofuram, and in particular chlorohydrocarbons, eg. methylene chloride and chloroform.
The reaction is carried out in general at, for example, from 0° to 100° C., preferably from 20° to 80° C. In the presence of a solvent, it is advantageously carried out at the boiling point of the particular solvent.
The novel starting compounds II are obtained, for example, by epoxidation of the corresponding olefins V ##STR6## (cf. G. Dittus in Houben-Weyl-Muller, Methoden der Organischen Chemie, Georg Thieme Verlag, Stuttgart, 1965, Vol. VI, 3, page 385 et seq.).
The compound V is prepared by halogenating or oxidizing olefins of the formula IX ##STR7## by know methods in the allyl position.
Suitable halogenating reagents are N-chloro- and N-bromosuccinimide in halohydrocarbons, such as carbon tetrachloride, trichloroethane or methylene chloride, temperatures of from 20° to 100° C. being employed. For the allyl oxidation, peresters, such as tert-butyl perbenzoate or tert-butyl peracetate, are used in the presence of a heavy metal salt, eg. copper(I) chloride or copper(I) bromide. The reaction is carried out in an inert solvent at from 10° to 100° C.
The allyl halides or alcohols V thus obtained are then converted into the corresponding epoxides II (L=halogen or OH). For this purpose, the olefins V are oxidized with a peroxycarboxylic acid, such as perbenzoic acid, 3-chloroperbenzoic acid, 4-nitroperbenzoic acid, monoperphthalic acid, peracetic acid, perpropionic acid, permaleic acid, monopersuccinic acid, perpelargonic acid or trifluoroperacetic acid, in an inert solvent, preferably a chlorohydrocarbon, eg. methylene chloride, chloroform, carbon tetrachloride or dichloroethane, or, if required, in acetic acid, ethyl acetate, acetone or dimethylformamide, in the presence or absence of a buffer, such as sodium acetate, sodium carbonate, disodium hydrogen phosphate or Triton B. The reaction is carried out at from 10° to 100° C. and, if required, is catalyzed with, for example, iodine, sodium tungstate or light. Alkaline solutions of hydrogen peroxide (about 30% strength) in methanol, ethanol, acetone or acetonitrile, at from 25° to 30° C., and alkyl hydroperoxides, eg. tert-butyl hydroperoxide, with the addition of a catalyst, eg. sodium tungstate, pertungstic acid, molybdenum hexacarbonyl or vanadyl acetylacetonate, are also suitable for the oxidation. Some of the state oxidizing agents can be produced in situ.
While the resulting epoxyhalides II (L=halogen) can be reacted immediately by process a), the corresponding epoxyalcohols II (L=OH) are converted into, for example, reactive esters, which are then reacted with the compounds III by process a).
The reactive esters which can be reacted with III are prepared by generally known methods (Houben-Weyl-Muller, Methoden der organischen Chemie, Georg Thieme Verlag, Stuttgart, 1955, Volume 9, pages 388, 663 and 671). Examples of such esters are methanesulfonates, trifluoromethanesulfonates, 2,2,2-trifluoroethanesulfonates, nonafluorobutanesulfonates, 4-methylbenzenesulfonates, 4-bromobenzenesulfonates, 4-nitrobenzenesulfonates and benzenesulfonates.
The compounds V can be prepared by generally known processes of olefin synthesis (Houben-Weyl-Muller, Methoden der organischen Chemie, Georg Thieme Verlag, Stuttgart, 1972, Vol. V, 1b).
The compounds of the formula IV ##STR8## are obtained, for example, by a) reacting a compound of the formula V ##STR9## where R1 and R2 have the abovementioned meanings and L is a leaving group which can be substituted by a nucleophile, with a compound of the formula III ##STR10## where Me is hydrogen, a metal atom or trimethylsilyl and X, Y and Z have the above mentioned meanings, or reacting a compound of the formula VI ##STR11## where R1, X, Y and Z have the abovementioned meanings, with a compound of the formula VII ##STR12## where R2 has the same meanings as in formula I and R3, R4 and R5 may be identical or different and are each phenyl, p-carboxyphenyl, p-dimethylaminophenyl, dimethylamino, piperidino, morpholino, alkyl of 1 to
3 carbon atoms or cyclohexyl.
The compounds of the formula I in which E is F, Cl or Br can be prepared, for example, by reacting a compound of the formula VIII ##STR13## where R1, R2 and D have the state meanings, with a compound of the formula III ##STR14## where X, Y, Z and Me have the abovementioned meanings, in the presence of a thionyl halide.
The reaction is carried out, for example, in the presence or absence of a solvent or diluent at from -30° to 80° C. The preferred solvents and diluents include nitriles, such as acetonitrile or, propionitrile, ethers, such as tetrahydrofuran, diethyl ether, dimethoxyethane, dioxane or diisopropyl ether, and in particular hydrocarbons and chlorohydrocarbons, such as pentane, hexane, toluene, methylene chloride, chloroform, carbon tetrachloride or dichloroethane, or mixtures of these.
The novel starting compounds VIII in which D is O are obtained, for example, by epoxidation of the corresponding olefins X ##STR15## (cf. G. Dittus in Houben-Weyl-Muller, Methoden der Organischen Chemie, Georg Thieme Verlag, Stuttgart, 1965, Vol. VI, 3, page 38 et seq.).
The compounds X can be prepared by generally known methods of aldehyde synthesis (Houben-Weyl-Muller, Methoden der Organischen Chemie, Georg Thieme Verlag, Stuttgart, 1983, Vol. E3).
The Examples which follow illustrate the preparation of the active ingredients.
8.4 g of sodium hydroxide in 40 ml of water are added to a solution of 85.5 g of 2-trifluoromethylbenzaldehyde in 300 ml of methanol. The reaction mixture is cooled to 10° C. and 69 g of 4-fluorophenylacetaldehyde are rapidly added dropwise, the temperature of the solution not exceeding 30° C. After stirring has been carried out for two hours at room temperature, 300 ml of water are added to the colorless reaction solution, and the resulting emulsion is extracted by shaking with methyl tert-butyl ether. The organic phase is separated off, dried over sodium sulfate and evaporated down under reduced pressure. In the subsequent distillation of the remaining residue, 96 g (65%) of E-2-(4-fluorophenyl)-3-(2-trifluoromethylphenyl)-propenal are obtained at 116° C./0.3 mbar.
96 g of E-2-(-4-fluorophenyl)-3-(2-trifluoromethylphenyl)-propenal are dissolved in 300 ml of methanol and 2.3 ml of concentrated sodium hydroxide solution are added. The reaction solution is stirred at 0° C. while 27.7 g of about 50% strength hydrogen peroxide are slowly added dropwise, the internal temperature not exceeding 30° C. After the end of the addition, stirring is continued for 6 hours at room temperature (20° C.), after which 5 g of sodium borohydride, which has been dissolved in a little 10% strength sodium hydroxide solution, are added. After the reaction mixture has been stirred for 18 hours at room temperature, 100 ml of water are added to the solution and the resulting emulsion is extracted by shaking with methylene chloride. The organic phase isolated is then dried over sodium sulfate and evaporated down. 90 g (89%) of cis-2-hydroxymethyl-2-(4-fluorophenyl)-3-(2-trifluoromethylphenyl)-oxirane are obtained.
61 g of 4-methlbenzenesulfonyl chloride are added to a solution of 90 g of cis-2-hydroxymethyl-2-(4-fluorophenyl)-3-(2-trifluoromethylphenyl)-oxirane in 300 ml of methylene chloride and 58 g of triethylamine at room temperature. After 24 hours, the reaction mixture is washed with aqueous sodium bicarbonate solution and water and evaporated down under reduced pressure. The residue gives 128.4 g (95%) of cis-2-(4-methylphenylsulfonyloxymethyl)-2-(4-fluorophenyl)-3-(2-trifluoromethylphenyl)-oxirane, which is then further processed with triazole.
7.3 g of sodium borohydride, which has been dissolved in a little 10% strength sodium hydroxide solution are added to a solution of 150 g of E-2-(4-fluorophenyl)-3-(2-chlorophenyl)-propenal (prepared as described in Example A) in 600 ml of isopropanol at 0° C. After the reaction mixture has been stirred for two hours at room temperature, 300 ml of water are added to the solution and the resulting emulsion is extracted by shaking with methylene chloride. The organic phase isolated is then dried over sodium sulfate and evaporated down. 150.7 g (100%) of E-2-(4-fluorophenyl)-3-(2-chlorophenyl)-prop-2-enol are obtained.
103.1 g of E-2-(4-fluoropehnyl)-3-(2-chlorophenyl)-prop-2-enol are dissolved in 700 ml of methyl tert-butyl ether, and 2 ml of pyridine are added. The reaction solution is stirred under a nitrogen atmosphere at 0° C., while 27.2 g of phosphorus tribromide are added in the course of 90 minutes. After the end of the addition, the mixture is refluxed for two hours and then poured onto 500 ml of water and extracted several times with methyl tert-butyl ether. The organic phase is washed with sodium bicarbonate solution and water and dried over sodium sulfate, and the solvent is evaporated down under reduced pressure. 77.2 g (61%) of E-1-bromo-2-(4-fluorophenyl)-3-(2-chlorophenyl)-prop-2-ene of melting point 68° C. are obtained from ethanol.
77.2 g of E-1-bromo-2-(4-fluorophenyl)-3-(2-chlorophenyl)-prop-2-ene are heated at 180° C. for one hour. The reaction mixture is cooled to room temperature and 200 ml of ethanol are added. Thereafter, 10 g of active carbon are added and the mixture is heated to 50° C. and filtered while hot. 26.9 g (35%) of Z-1-bromo-2-(4-fluorophenyl)-3-(2-chlorophenyl)-prop-2-ene of melting point 73°-75° C. are obtained from ethanol.
78.2 g of E-2-(4-fluorophenyl)-3-(2-chlorophenyl)-propenal are dissolved in 300 ml of methanol, and 1 ml of concentrated sodium hydroxide solution is added. The reaction solution is stirred at 0° C. while 20.5 g of about 50% strength hydrogen peroxide are slowing added dropwise, the internal temperature not exceeding 30° C. After the end of the addition, the mixture is stirred for six hours at room temperature, after which 100 ml of water are added and the resulting emulsion is extracted by shaking with methyl tert-butyl ether. The organic phase isolated is then dried over sodium sulfate and evaporated down. 52.5 g (63%) of cis-2-formyl-2-(4-fluorophenyl)-3-(2-chlorophenyl)-oxirane are obtained.
55 g of 4,5-dichloroimidazole and 9.5 g of sodium hydride (80% strength dispersion in mineral oil) are suspended in 300 ml of N,N-dimethylformamide and a solution of 128.4 g of cis-2-(4-methylphenylsulfonyloxymethyl)-2-(4-fluorophenyl)-3-(2-trifluoromethylphenyl) -oxirane in 200 ml of N,N-dimethylformamide is added at room temperature. After eight hours, the reaction solution is poured onto water and extracted with methyl tert-butyl ether. The organic phase is washed with water and dried over sodium sulfate and the solvent is evaporated down under reduce pressure. 86.4 g (76%) of cis-2-(4,5-dichloroimidazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-trifluoromethylphenyl)-oxirane of melting point 158° C. (compound) No. 1) are obtained from methyl tert-butyl ether/n-hexane.
The compounds listed in Table 1 can be prepared similarly to Example 1.
15 g of 5-nitroimidazole and 31 g of potassium carbonate are added to a solution of 7.5 g of Z-1-bromo-2-(4-fluorophenyl)-3-(2-chlorophenyl)-prop-2-ene in 40 ml of dimethylformamide. After the reaction mixture has been stirred for 24 hours at room temperature, 50 ml of water are added and the mixture is extracted several times with methyl tert-butyl ether; the organic phase is washed with water, dried over sodium sulfate and evaporated down under reduced pressure. 6.7 g (81%) of Z-1-(5-nitroimidazol-1-yl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)-prop-2-ene of melting point 161°-165° C. (compound No. 1a) are obtained from methyl tert-butyl ether/n-hexane.
The compounds listed in Table 2 can be prepared similarly to Example 2.
13.1 g of thionyl chloride are added to a solution of 27.7 g of methyl 4-imidazolecarboxylate in 150 ml of methylene chloride at 0° C. After the end of the addition, the mixture is stirred for 30 minutes at room temperature and 18.5 g of cis-2-formyl-2-(4-fluorophenyl)-3-(2-chlorophenyl)-oxirane are then added. After the reaction mixture has been stirred for 12-15 hours at room temperature, 100 ml of water are added to the solution and the organic phase is separated off. The remaining aqueous phase is extracted twice by shaking with methylene chloride and the collected organic phases are washed twice with saturated sodium bicarbonate solution. The organic phase isolated is then dried over sodium sulfate and evaporated down. 14.3 g (53%) of cis-2-[1-(4-methoxycarbonylimidazol-1-yl)-1-chloromethyl]-2-(4-fluorophenyl)-3-(2-chlorophenyl)-oxirane of melting point 199°-203° C. (compound No. 25) are obtained from methyl tert-butyl ether.
The compounds listed is Table 1 can be prepared similarly to Example 3.
13.1 g of thionyl chloride are added to a solution of 30.1 g of 4,5-dichloroimidazole in 150 ml of methylene chloride at 0° C. After the end of the addition, the mixture is stirred for 30 minutes at room temperature and 17.4 g of E-2-(4-fluorophenyl)-3-(2-chlorophenyl)-propenal are then added. After the reaction mixture has been stirred for 12-15 hours at room temperature, 100 ml of water are added to the solution and the organic phase is separated off. The remaining aqueous phase is extracted twice by shaking with methylene chloride and the collected organic phases are washed twice with saturated sodium bicarbonate solution. The organic phase isolated is then dried over sodium sulfate and evaporated down, and the residue is purified by chromatography over silica gel using 9:1 ethyl acetate n-hexane. 24.8 (89%) of E-1-chloro-1-(4,5-dichloroimidazol-1-yl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)-prop-2-ene (compound No. 8a) are obtained.
The compounds listed in Table 2 can be prepared similarly to Example 4.
TABLE 1
__________________________________________________________________________
##STR16##
Ex. R.sup.1 R.sup.2 E X Y Z m.p./IR Isomer
__________________________________________________________________________
1 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H Cl Cl H 158° C.
cis
2 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H 1699, 1514, 1315
cis
1222, 1123, 771, cm.sup.-1
3 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H Cl CH.sub.3
H 164-167° C.
cis
4 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H H CH.sub.3
5 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H CN H
6 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H NO.sub.2
H H
7 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H CH.sub.3
H
8 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
Cl Cl H
9 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
10 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
11 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
H H CH.sub.3
12 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
H CN H
13 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
NO.sub.2
H H
14 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Br
Cl Cl H
15 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
16 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Br
H CH.sub.3
H
17 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl Cl H 108-115° C.
cis
18 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H resin cis
19 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl CH.sub.3
H 112-113° C.
cis
20 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H H CH.sub.3
100-103° C.
cis
21 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H CN H 128-131° C.
cis
22 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H NO.sub.2
H 206-208° C.
cis
23 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H CH.sub.3
H resin cis
24 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H 156-158° C.
cis
25 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H 199-203° C.
cis
26 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H 146-156° C.
D1:D2 = 1:1
27 4-FC.sub.6 H.sub. 4
2-ClC.sub.6 H.sub.4
Cl
H H CH.sub.3
28 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
H CN H 50-60° C.
D1:D2 = 2:1
29 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
NO.sub.2
H H
30 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
H CH.sub.3
H
31 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
Cl Cl H 115-122° C.
D1:D2 = 4:1
32 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H 162° C.
cis
33 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
Cl CH.sub.3
H
34 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
H H CH.sub.3
35 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
H CN H
36 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
NO.sub.2
H H
37 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H Cl Cl H 146-148° C.
cis
38 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H 138-141° C.
cis
39 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H Cl CH.sub.3
H 124-126° C.
cis
40 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H H H CH.sub.3
41 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H H CN H
42 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H NO.sub.2
H H
43 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H H COCH.sub.3
H 127-130° C.
cis
44 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
45 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
46 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
47 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
H H CH.sub.3
48 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
H CN H
49 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
NO.sub.2
H H
50 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
Cl Cl H
51 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
52 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
Cl CH.sub.3
H
53 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
H H CH.sub.3
54 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
H CN H
55 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
NO.sub.2
H H
56 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
H CH.sub.3
H
57 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
H Cl Cl H 105-110° C.
cis
58 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H resin cis
59 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
H Cl CH.sub.3
H 150° C.
cis
60 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
H H H CH.sub.3
61 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub. 3
H H CN H
62 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
H NO.sub.2
H H
63 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
H H CH.sub.3
H
64 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
Cl Cl H 145-149° C.
D1:D2 = 2:1
65 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
66 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
Cl CH.sub.3
H
67 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
H H CH.sub.3
68 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
H CN H
69 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
NO.sub.2
H H
70 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
H CH.sub.3
H
71 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Br
Cl Cl H
72 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
73 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub. 3
Br
Cl CH.sub.3
H
74 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Br
H H CH.sub.3
75 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Br
H CN H
76 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Br
NO.sub.2
H H
77 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Br
H CH.sub.3
H
78 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
79 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
80 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl CH.sub.3
H
81 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Cl
Cl Cl H
82 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
83 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
84 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Br
Cl Cl H
85 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
86 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Br
H CH.sub.3
H
87 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H Cl Cl H
88 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
89 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H Cl CH.sub.3
H
90 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H H CH.sub.3
H
91 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
Cl Cl H
92 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
93 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
94 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
H CH.sub.3
H
95 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Br
Cl Cl H
96 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
97 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Br
Cl CH.sub.3
H
98 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Br
H CH.sub.3
H
99 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
H Cl Cl H resin cis
100 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H 141-144° C.
cis
101 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
H Cl CH.sub.3
H 144-147° C.
cis
102 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
H H COCH.sub.3
H resin cis
103 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
H H H CH.sub.3
104 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H 1607, 1507, 1463,
D.sub.1 :D.sub.2 = 2:1
1237, 964 cm.sup.-1
105 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
106 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Cl
Cl CH.sub.3
H
107 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Cl
H CH.sub.3
H
108 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Cl
H H CH.sub.3
109 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Br
Cl Cl H
110 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
111 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Br
Cl CH.sub.3
H
112 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
H Cl Cl H 131-132° C.
cis
113 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H resin cis
114 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
H Cl CH.sub.3
H 129-132° C.
cis
115 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
H H COCH.sub.3
H resin cis
116 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
117 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Cl
Cl CH.sub.3
H
118 4-FC.sub.6 H.sub.4
2,6-F.sub.2 C.sub.6 H.sub.3
Br
Cl Cl H
119 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
120 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Br
H H CH.sub.3
121 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
H Cl Cl H
122 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H
123 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
H Cl CH.sub.3
H
124 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H
125 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
126 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
Cl CH.sub.3
H
127 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Br
Cl Cl H
128 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
129 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Br
Cl CH.sub.3
H
130 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H Cl Cl H
131 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H 1731, 1514, 1494,
cis
1245, 1223, 758 cm.sup.-1
132 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H Cl CH.sub.3
H
133 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H H CH.sub.3
H
134 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H H H CH.sub.3
135 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H H CN H
136 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H NO.sub.2
H H
137 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Cl
Cl Cl H 146-149° C.
cis
138 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
139 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
140 4-FC.sub.6 H.sub.4
2-OCH.sub. 3C.sub.6 H.sub.4
Cl
H CH.sub.3
H
141 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Cl
H H CH.sub.3
142 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Cl
H CN H
143 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Cl
NO.sub.2
H H
144 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Br
Cl Cl H resin D1:D2 = 3:1
145 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
146 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Br
Cl CH.sub.3
H
147 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
H Cl Cl H
148 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
149 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
H Cl CH.sub.3
H
150 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
H H CH.sub.3
H
151 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
H H H CH.sub.3
152 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
H H CN H
153 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Cl
Cl Cl H
154 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
155 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
156 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Cl
H CH.sub.3
H
157 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Br
Cl Cl H
158 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
159 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Br
Cl CH.sub.3
H
160 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Br
H CH.sub.3
H
161 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
H Cl Cl H 125-128° C.
cis
162 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
H H CO.sub.2 CH.sub.3
H 116-120° C.
cis
163 4-F C.sub.6 H.sub.4
C.sub.6 H.sub.5
H Cl CH.sub.3
H
164 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
H H CH.sub.3
H
165 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Cl
Cl Cl H
166 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Cl
H CO.sub.2 CH.sub.3
H
167 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Cl
Cl CH.sub.3
H
168 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Cl
H CH.sub.3
H
169 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Br
Cl Cl H
170 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Br
H CO.sub.2 CH.sub.3
H
171 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Br
Cl CH.sub.3
H
172 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Br
H CH.sub.3
H
173 4-FC.sub.6 H.sub.4
cyclohexyl
H Cl Cl H 2929, 1513, 1253,
cis
837 cm.sup.-1
174 4-FC.sub.6 H.sub.4
cyclohexyl
H H CO.sub.2 CH.sub.3
H
175 4-FC.sub.6 H.sub.4
cyclohexyl
H Cl CH.sub. 3
H
176 4-FC.sub.6 H.sub.4
cyclohexyl
Cl
Cl Cl H
177 4-FC.sub.6 H.sub.4
cyclohexyl
Cl
H CO.sub.2 CH.sub.3
H
178 4-FC.sub.6 H.sub.4
cyclohexyl
Cl
Cl CH.sub.3
H
179 4-FC.sub.6 H.sub.4
cyclohexyl
Br
Cl Cl H
180 4-FC.sub.6 H.sub.4
cyclohexyl
Br
H CO.sub.2 CH.sub.3
H
181 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
H Cl Cl H 124-128° C.
cis
182 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H resin cis
183 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
H Cl CH.sub.3
H 142° C.
cis
184 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
H H H CH.sub.3
89-90° C.
cis
185 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
H H CN H 105-110° C.
cis
186 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
H NO.sub.2
H H 200° C.
cis
187 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
H H CH.sub.3
H 91-95° C.
cis/trans = 1.5:1
188 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H
189 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
190 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
191 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
Br
Cl Cl H
192 C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
193 C.sub.6 H.sub.5
C.sub.6 H.sub.5
H Cl Cl H
194 C.sub.6 H.sub.5
C.sub.6 H.sub.5
H H CO.sub.2 CH.sub.3
H
195 C.sub.6 H.sub.5
C.sub.6 H.sub.5
Cl
Cl Cl H
196 C.sub.6 H.sub.5
C.sub.6 H.sub.5
Cl
H CO.sub.2 CH.sub.3
H
197 C.sub.6 H.sub.5
C.sub.6 H.sub.5
Br
Cl Cl H
198 C.sub.6 H.sub.5
C.sub.6 H.sub.5
Br
H CO.sub.2 CH.sub.3
H
199 C.sub.6 H.sub.5
4-ClC.sub.6 H.sub.4
H Cl Cl H
200 C.sub.6 H.sub.5
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
201 C.sub.6 H.sub.5
4-Cl C.sub.6 H.sub.4
Br
Cl Cl H
202 C.sub.6 H.sub.5
2,4-Cl.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H
203 C.sub.6 H.sub.5
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H
204 C.sub.6 H.sub.5
2,4-Cl.sub.2C.sub.6 H.sub.3
Br
Cl CH.sub.3
H
205 C.sub.6 H.sub.5
4-NO.sub.2C.sub.6 H.sub.4
H Cl Cl H
206 C.sub.6 H.sub.5
3-NO.sub.2C.sub.6 H.sub.4
H H CH.sub.3
H
207 C.sub.6 H.sub.5
cyclohexyl
H CH.sub.3
Cl H
208 4-ClC.sub.6 H.sub.4
C.sub.6 H.sub.5
H Cl Cl H
209 4-ClC.sub.6 H.sub.4
C.sub.6 H.sub.5
Cl
Cl Cl H
210 4-ClC.sub.6 H.sub.4
C.sub.6 H.sub.5
Br
H CH.sub.3
H
211 4-ClC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H Cl Cl H
212 4-ClC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
213 4-ClC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
H H CH.sub.3
214 4-ClC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
H Cl Cl H
215 4-ClC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H
216 4-ClC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
Cl Cl H
217 4-ClC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H Cl Cl H
218 4-ClC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
219 4-ClC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
220 4-ClC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Cl
Cl Cl H
221 2-ClC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl Cl H
222 2-ClC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H
223 2-ClC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
H CH.sub.3
H
224 2-ClC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
225 2-ClC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Cl
Cl Cl H
226 2-ClC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H Cl Cl H
227 2-ClC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
228 2-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl Cl H 87-94° C.
cis:trans = 3:1
229 2-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
H CH.sub.3
H
230 2-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H Cl Cl H
231 2-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
Cl Cl H
232 2-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H Cl Cl H
233 2-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
234 2,4-Cl.sub.2C.sub.6 H.sub.3
2-ClC.sub.6 H.sub.4
H H CH.sub.3
H
235 2,4-Cl.sub.2C.sub.6 H.sub.3
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H
236 2,4-Cl.sub.2C.sub.6 H.sub.3
4-ClC.sub.6 H.sub.4
H H H CH.sub.3
237 2,4-Cl.sub.2C.sub.6 H.sub.3
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
238 2,4-Cl.sub.2C.sub.6 H.sub.3
2,4-Cl.sub.2C.sub.6 H.sub.3
H Cl Cl H
239 2,4-Cl.sub.2C.sub.6 H.sub.3
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H
240 2,4-Cl.sub.2C.sub.6 H.sub.3
4-FC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
241 2,4-Cl.sub.2C.sub.6 H.sub.3
4-FC.sub.6 H.sub.4
Br
Cl CH.sub.3
H
242 cyclohexyl
C.sub.6 H.sub.5
H Cl Cl H
243 cyclohexyl
C.sub.6 H.sub.5
Cl
H CN H
244 cyclohexyl
C.sub.6 H.sub.5
Br
H H CH.sub.3
245 cyclohexyl
2-ClC.sub.6 H.sub.4
H Cl Cl H
246 cyclohexyl
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H
247 cyclohexyl
2-ClC.sub.6 H.sub.4
Br
H CH.sub.3
H
248 cyclohexyl
4-ClC.sub.6 H.sub.4
H Cl Cl H
249 cyclohexyl
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
250 cyclohexyl
2,4-Cl.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H
251 cyclohexyl
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
252 cyclohexyl
2-FC.sub.6 H.sub.4
H H CH.sub.3
H
253 cyclohexyl
2-FC.sub.6 H.sub.4
Cl
NO.sub.2
H H
254 cyclohexyl
4-FC.sub.6 H.sub.4
H Cl Cl H
255 cyclohexyl
4-FC.sub.6 H.sub.4
Cl
Cl Cl H
256 cyclohexyl
4-FC.sub.6 H.sub.4
Br
Cl Cl H
257 cyclohexyl
2-Cl-4-FC.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H
258 cyclohexyl
2-Cl-4-FC.sub.6 H.sub.3
Cl
Cl Cl H
259 cyclohexyl
2-Cl-4-FC.sub.6 H.sub.3
Br
Cl CH.sub.3
H
260 tert.-C.sub.4 H.sub.9
C.sub.6 H.sub.5
H H H CH.sub.3
261 tert.-C.sub.4 H.sub.9
C.sub.6 H.sub.5
Cl
Cl Cl H
262 tert.-C.sub.4 H.sub.9
2-ClC.sub.6 H.sub.4
H Cl Cl H
263 tert.-C.sub.4 H.sub.9
2-ClC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
264 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
H Cl Cl H
265 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
266 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
H Cl CH.sub.3
H
267 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
H H CH.sub.3
H
268 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
H H H CH.sub.3
269 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
270 tert.-C.sub.4 H.sub. 9
4-ClC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
271 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
272 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
Cl
H CH.sub.3
H
273 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
Cl
H H CH.sub.3
274 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
Br
Cl Cl H
275 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
276 tert.-C.sub.4 H.sub.9
4-ClC.sub.6 H.sub.4
Br
Cl CH.sub.3
H
277 2,4-Cl.sub.2C.sub.6 H.sub.3
2-ClC.sub.6 H.sub.4
H Cl Cl H
278 2,4-Cl.sub.2C.sub.6 H.sub.3
2-ClC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
279 2,4-Cl.sub.2C.sub.6 H.sub.3
4-ClC.sub.6 H.sub.4
H Cl Cl H
280 2,4-Cl.sub.2C.sub.6 H.sub.3
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
281 2,4-Cl.sub.2C.sub.6 H.sub.3
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H
282 2,4-Cl.sub.2C.sub.6 H.sub.3
2,4-Cl.sub.2C.sub.6 H.sub. 3
H H CH.sub.3
H
283 2,4-Cl.sub.2C.sub.6 H.sub.3
4-FC.sub.6 H.sub.4
H Cl CH.sub.3
H
284 2,4-Cl.sub.2C.sub.6 H.sub.3
2-FC.sub.6 H.sub.4
H H H CH.sub.3
285 4-BrC.sub.6 H.sub.4
4-C(CH.sub.3).sub.3C.sub.6 H.sub.4
H H CH.sub.3
H
286 2-OCH.sub.3C.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl Cl H
287 2-OCH.sub.3C.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
288 2-OCH.sub.3C.sub.6 H.sub.4
2-C.sub.10 H.sub.7
H Cl Cl H
289 2-OCH.sub.3C.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
290 2-OCH.sub.3C.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
291 2-C.sub.10 H.sub.7
2-ClC.sub.6 H.sub.4
H Cl Cl H
292 2-C.sub.10 H.sub.7
4-FC.sub.6 H.sub.4
Cl
Cl Cl H
293 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H COCH.sub.3
CH.sub.3
130-131° C.
cis
294 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
H COCH.sub.3
CH.sub.3
295 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
H COCH.sub.3
CH.sub.3
296 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
F Cl Cl H
297 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
F Cl CH.sub.3
H
298 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
F Cl Cl H
299 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
F H CN H
300 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
F Cl Cl H
301 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
F Cl CH.sub.3
H
302 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
F Cl Cl H
303 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
F H CN H
304 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
F Cl CH.sub.3
H
305 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
F Cl Cl H
306 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
F Cl Cl H
307 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
F H COCH.sub.3
CH.sub.3
308 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
F Cl Cl H
309 4-FC.sub.6 H.sub.4
4-OCH.sub.3C.sub.6 H.sub.4
F H CN H
310 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
F Cl CH.sub.3
H
311 4-FC.sub.6 H.sub.4
cyclohexyl
F Cl Cl H
312 C.sub.6 H.sub.5
4-ClC.sub.6 H.sub.4
F Cl Cl H
313 4-ClC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
F Cl CH.sub.3
H
314 cyclohexyl
4-FC.sub.6 H.sub.4
F Cl Cl H
315 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H COCH.sub.3
H resin cis
316 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H COCH.sub.3
CH.sub.3
H 136-141° C.
cis
317 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H phenyl
H resin D1:D2 = 2:1
318 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H H phenyl
319 4-FC.sub.6 H.sub.4
C.sub.6 H.sub. 5
H H CN H 126-130° C.
cis
320 4-FC.sub.6 H.sub.4
2-F-3ClC.sub.6 H.sub.3
H Cl Cl H 150-153° C.
cis
321 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H resin cis
322 C.sub.6 H.sub.5
2-OCH.sub.3C.sub.6 H.sub.4
H Cl Cl H resin cis
323 4-FC.sub.6 H.sub.4
2-BrC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H resin cis
324 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H CO.sub.2 CH.sub.3
CO.sub.2 CH.sub.3
H 134-140° C.
cis
__________________________________________________________________________
TABLE 2
__________________________________________________________________________
##STR17##
Ex. R.sup.1
R.sup.2 E X Y Z m.p./IR Isomer
__________________________________________________________________________
1a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H NO.sub.2
H H 161-165° C.
Z
2a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H 132-135° C.
Z
3a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl Cl H 84-89° C.
Z
4a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H CN H 99-108° C.
Z/E = 6:1
5a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl CH.sub.3
H resin Z/E = 3:2
6a 4-FC.sub.6 H.sub.4
2-Cl C.sub.6 H.sub.4
H H H CH.sub.3
1603, 1509, 1228
Z
846, 830, 759 cm.sup.-1
7a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H H CH.sub.3
H 93-95° C.
Z
8a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H 1603, 1510, 1470,
E
1233, 847, 753 cm.sup.-1
9a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
10a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
Cl Cl H 172-175° C.
E
11a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Br
Cl CH.sub.3
H
12a 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
H Cl Cl H
13a 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
14a 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
Cl Cl H
15a 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H
16a 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
17a 4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
18a 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
H Cl Cl H
19a 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Cl
Cl Cl H
20a 4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
Br
Cl Cl H
21a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H NO.sub.2
H H
22a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
23a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H Cl Cl H 1604, 1561, 1316,
E/Z = 2:1
1126, 768 cm.sup.-1
24a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H CN H
25a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H Cl CH.sub.3
H 1510, 1316, 1167
E/ = 2:1
1123, 769 cm.sup.-1
26a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H H CH.sub.3
27a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
H H CH.sub.3
H
28a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
Cl Cl H
29a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
30a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Cl
Cl CH.sub.3
H
31a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Br
Cl Cl H
32a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Br
Cl CH.sub.3
H
33a 4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
34a 4-FC.sub.6 H.sub.4
4-CF.sub.3C.sub.6 H.sub.4
H Cl Cl H
35a 4-FC.sub.6 H.sub.4
4-CF.sub.3C.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
36a 4-FC.sub.6 H.sub.4
4-CF.sub.3C.sub.6 H.sub.4
Br
Cl CH.sub.3
H
37a 4-FC.sub.6 H.sub. 4
2-FC.sub.6 H.sub.4
H Cl Cl H
38a 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl CH.sub.3
H
39a 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Cl
Cl Cl H
40a 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
41a 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Br
Cl Cl H
42a 4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
Br
Cl CH.sub.3
H
43a 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H Cl Cl H
44a 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H
45a 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
Cl Cl H
46a 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Cl
H CO.sub.2 CH.sub.3
H
47a 4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Br
Cl Cl H
48a 4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
49a 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub. 3
H Cl Cl H
50a 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H
51a 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H
52a 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
53a 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Br
Cl Cl H
54a 4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
55a 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
H Cl Cl H
56a 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
H H CO.sub.2 CH.sub.3
H
57a 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Cl
Cl Cl H
58a 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Cl
H CO.sub.2 CH.sub.3
H
59a 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Br
Cl Cl H
60a 4-FC.sub.6 H.sub.4
2,6-F.sub.2C.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
61a 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H Cl Cl H resin E/Z = 3:1
62a 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H Cl CH.sub.3
H 1599, 1509,
E/Z = 3:1
1248, 1225,
754 cm.sup.-1
63a 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H H CN H resin E/Z = 3:1
64a 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H H CH.sub.3
H 1599, 1509, 1247,
E/Z = 3:1
754 cm.sup.-1
65a 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
H H CO.sub.2 CH.sub.3
H 1720, 1509, 1248,
E/Z = 3:1
1116, 755 cm.sup.-1
66a 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Cl
Cl Cl H
67a 4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.4
Br
H CO.sub.2 CH.sub.3
H
68a 4-FC.sub.6 H.sub.4
4-OCF.sub.3 C.sub.6 H.sub.4
H Cl Cl H
69a 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Cl
Cl Cl H
70a 4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
Br
Cl Cl H
71a 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
H Cl Cl H
72a 4-FC.sub.6 H.sub.4
C.sub.6 H.sub.5
Cl
H CO.sub.2 CH.sub.3
H
73a 4-FC.sub.6 H.sub.4
cyclohexyl
H Cl Cl H
74a 4-FC.sub.6 H.sub.4
cyclohexyl
Cl
H CH.sub.3
H
75a C.sub.6 H.sub.5
C.sub.6 H.sub.5
H Cl Cl H
76a C.sub.6 H.sub.5
C.sub.6 H.sub.5
Cl
H H CH.sub.3
77a C.sub.6 H.sub.5
C.sub.6 H.sub.5
Br
H CO.sub.2 CH.sub.3
H
78a C.sub.6 H.sub.5
4-ClC.sub.6 H.sub.4
H Cl Cl H
79a C.sub.6 H.sub.5
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H
80a C.sub.6 H.sub.5
2,4-Cl.sub.2C.sub.6 H.sub.3
Br
H CO.sub.2 CH.sub.3
H
81a C.sub.6 H.sub.5
4-FC.sub.6 H.sub.4
H Cl Cl H
82a C.sub.6 H.sub.5
2-FC.sub.6 H.sub.4
H Cl Cl H
83a 4-ClC.sub.6 H.sub.4
C.sub.6 H.sub.5
H Cl Cl H
84a 4-ClC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl Cl H
85a 4-ClC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
Cl
Cl Cl H
86a 4-ClC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
Br
H CH.sub.3
H
87a 4-ClC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H Cl Cl H
88a 4-ClC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
89a 2-ClC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
H Cl Cl H
90a 2-ClC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
91a 2-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
92a 2-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
H Cl Cl H
93a 2-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
Br
Cl Cl H
94a 2-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
H Cl Cl H
95a cyclohexyl
2-ClC.sub.6 H.sub.4
H Cl Cl H
96a cyclohexyl
4-ClC.sub.6 H.sub.4
Cl
Cl Cl H
97a cyclohexyl
4-FC.sub.6 H.sub.4
H Cl Cl H
98a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
F CH.sub.3
Cl H
99a 4-FC.sub.6 H.sub.4
2-ClC.sub.6 H.sub.4
F Cl Cl H
100a
4-FC.sub.6 H.sub.4
4-ClC.sub.6 H.sub.4
F H CN H
101a
4-FC.sub.6 H.sub.4
2,4-Cl.sub.2C.sub.6 H.sub.3
F H CN H
102a
4-FC.sub.6 H.sub.4
2-Cl-4-FC.sub.6 H.sub.3
F Cl Cl H
103a
4-FC.sub.6 H.sub.4
2-CF.sub.3C.sub.6 H.sub.4
F CH.sub.3
Cl H
104a
4-FC.sub.6 H.sub.4
4-CF.sub.3C.sub.6 H.sub.4
F Cl Cl H
105a
4-FC.sub.6 H.sub.4
2-FC.sub.6 H.sub.4
F H CH.sub.3
H
106a
4-FC.sub.6 H.sub.4
4-FC.sub.6 H.sub.4
F Cl Cl H
107a
4-FC.sub.6 H.sub.4
2,4-F.sub.2C.sub.6 H.sub.3
F H CO.sub.2 CH.sub.3
H
108a
4-FC.sub.6 H.sub.4
2-OCH.sub.3C.sub.6 H.sub.3
F H CO.sub.2 CH.sub.3
H
109a
4-FC.sub.6 H.sub.4
4-OCF.sub.3C.sub.6 H.sub.4
F Cl Cl H
110a
C.sub.6 H.sub.5
4-ClC.sub.6 H.sub.4
F Cl Cl H
__________________________________________________________________________
Generally speaking, the novel compounds are extremely effective on a broad spectrum of phytopathogenic fungi, in particular those from the Ascomycetes and Basidiomycetes classes. Some of them have a systemic action and can be used as foliar and soil fungicides.
The fungicidal compounds are of particular interest for controlling a large number of fungi in various crops or their seeds, especially wheat, rye, barley, oats, rice, Indian corn, lawns, cotton, soybeans, coffee, sugar cane, fruit and ornamentals in horticulture and viticulture, and in vegetables such as cucumbers, beans and cucurbits.
The novel compounds are particularly useful for controlling the following plant diseases:
Erysiphe graminin in cereals,
Perysiphe cichoracearum and Sphaerotheca fuliginea in cucurbits,
Podosphaera leucotricha in apples,
Uncinula necator in vines,
Puccinia species in cereals,
Rhizoctonia species in cotton and lawns,
Ustilago species in cereals and sugar cane,
Venturia inaequalis (scab) in apples,
Helminthosporium species in cereals,
Septoria nodorum in wheat,
Botrytis cinerea (gray mold) in strawberries and grapes,
Cercospora arachidicola in groundnuts,
Pseudocercosporella herpotrichoides in wheat and barley,
Pyricularia oryzae in rice,
Phytophthora infestans in potatoes and tomatoes,
Fusarium and Verticillium species in various plants,
Plasmopara viticola in grapes,
Alternaria species in fruit and vegetables.
The compounds are applied by spraying or dusting the plants with the active ingredients, or treating the seeds of the plants with the active ingredients. They may be applied before or after infection of the plants or seeds by the fungi.
The novel substances can be converted into conventional formulations such as solutions, emulsions, suspensions, dusts, powders, pastes and granules. The application forms depend entirely on the purposes for which they are intended; they should at all events ensure a fine and uniform distribution of the active ingredient. The formulations are produced in known manner, for example by extending the active ingredient with solvents and/or carriers, with or without the use of emulsifiers and dispersants; if water is used as solvent, it is also possible to employ other organic solvents as auxiliary solvents. Suitable auxiliaries for this purpose are solvents such as aromatics (e.g., xylene), chlorinated aromatics (e.g., chlorobenzenes), paraffins (e.g., crude oil fractions), alcohols (e.g., methanol, butanol), ketones (e.g., cyclohexanone), amines (e.g., ethanolamine, dimethylformamide), and water; carriers such as ground natural minerals (e.g., kaolins, aluminas, talc and chalk) and ground synthetic minerals (e.g., highly disperse silica and silicates); emulsifiers such as nonionic and anionic emulsifiers (e.g., polyoxyethylene fatty alcohol ethers, alkyl sulfonates and aryl sulfonates); and dispersants such as lignin, sulfite waste liquors and methylcellulose.
The fungicidal agents generally contain from 0.1 to 95, and preferably from 0.5 to 90, wt % of active ingredient. The application rates are from 0.02 to 3 kg or more of active ingredient per hectare, depending on the type of effect desired. The novel compounds may also be used for protecting materials, for example against Paecilomyces variotii.
The agents and the ready-to-use formulations prepared from them such as solutions, emulsions, suspensions, powders, dusts, pastes and granules, are applied in conventional manner, for example by spraying, atomizing, dusting, scattering, dressing or watering.
Examples of formulations are given below.
I. 90 parts by weight of compound no. 113 is mixed with 10 parts by weight of N-methyl-α-pyrrolidone. A mixture is obtained which is suitable for application in the form of very fine drops.
II. 20 parts by weight of compound no. 115 is dissolved in a mixture consisting of 80 parts by weight of xylene, 10 parts by weight of the adduct of 8 to 10 moles of ethylene oxide and 1 mole of oleic acid-N-monethanolamide, 5 parts by weight of the calcium salt of dodecylbenzenesulfonic acid, and 5 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into water and uniformly distributing it therein, an aqueous dispersion is obtained.
III. 20 parts by weight of compound no 113 is dissolved in a mixture consisting of 40 parts by weight of cyclohexanone, 30 parts by weight of isobutanol, 20 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into water and finely distributing it therein, an aqueous dispersion is obtained.
IV. 20 parts by weight of compound no 115 is dissolved in a mixture consisting of 25 parts by weight of cyclohexanol, 65 parts by weight of a mineral oil fraction having a boiling point between 210° and 280° C., and 10 parts by weight of the adduct of 40 moles of ethylene oxide and 1 mole of castor oil. By pouring the solution into water and uniformly distributing it therein, an aqueous dispersion is obtained.
V. 80 parts by weight of compound no. 113 is well mixed with 3 parts by weight of the sodium salt of diisobutylnaphthalene-α-sulfonic acid, 10 parts by weight of the sodium salt of a lignin-sulfonic acid obtained from a sulfite waste liquor, and 7 parts by weight of powdered silica gel, and triturated in a hammer mill. By uniformly distributing the mixture in water, a spray liquor is obtained.
VI. 3 parts by weight of compound no. 115 is intimately mixed with 97 parts by weight of particulate kaolin. A dust is obtained containing 3% by weight of the active ingredient.
VII. 30 parts by weight of compound no. 113 is intimately mixed with a mixture consisting of 92 parts by weight of powdered silica gel and 8 parts by weight of paraffin oil which has been sprayed onto the surface of this silica gel. A formulation of the active ingredient is obtained having good adherence.
VIII. 40 parts by weight of compound no. 115 is intimately mixed with 10 parts of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate, 2 parts of silica gel and 48 parts of water to give a stable aqueous dispersion. Dilution in water gives an aqueous dispersion.
IX. 20 parts by weight of compound no. 113 is intimately mixed with 2 parts by weight of the calcium salt of dodecylbenzenesulfonic acid, 8 parts by weight of a fatty alcohol polyglycol ethr, 2 parts by weight of the sodium salt of a phenolsulfonic acid-urea-formaldehyde condensate and 68 parts by weight of a paraffinic mineral oil. A stable oily dispersion is obtained.
In these application forms, the agents according to the invention may also be present together with other active ingredients, for example herbicides, insecticides, growth regulators, and fungicides, and may furthermore be mixed and applied together with fertilizers. Admixture with other fungicides frequently results in an increase in the fungicidal spectrum.
The following list of fungicides with which the novel compounds may be combined is intended to illustrate possible combinations but not to impose any restrictions.
Examples of fungicides which may be combined with the novel compounds are;
sulfur,
dithiocarbamates and their derivatives, such as
ferric dimethyldithiocarbamate,
zinc dimethyldithiocarbamate,
zinc ethylenebisdithiocarbamate,
manganese ethylenebisdithiocarbamate,
manganese zinc ethylenediaminebisdithiocarbamate,
tetramethylthiuram disulfides,
ammonia complex of zinc N,N'-ethylenebisdithiocarbamate,
ammonia complex of zinc N,N'-propylenebisdithiocarbamate,
zinc N,N'-propylenebisdithiocarbamate and
N,N'-polypropylenebis(thiocarbamyl) disulfide;
nitro derivatives, such as
dinitro(1-methylheptyl)-phenyl crotonate,
2-sec-butyl-4,6-dinitrophenyl 3,3-dimethylacrylate,
2-sec-butyl-4,6-dinitrophenyl isopropylcarbonate and
diisopropyl 5-nitroisophthalate;
heterocyclic substances, such as
2-heptadecylimidazol-2-yl acetate,
2,4-dichloro-6-(o-chloroanilino)-s-triazine,
O,O-diethyl phthalimidophosphonothiote,
5-amino-1-[-bis-(dimethylamino)-phosphinyl]-3-phenyl-1,2,4-triazole,
2,3-dicyano-1,4-dithioanthraquinone,
2-thio-1,3-dithio[4,5-b]quinoxaline,
methyl 1-(butylcarbamyl)-2-benzimidazolecarbamate,
2-methoxycarbonylaminobenzimidazole,
2-(fur-2-yl)-benzimidazole,
2-(thiazol-4-yl)benzimidazole,
N-(1,1,2,2-tetrachloroethylthio)-tetrahydrophthalimide,
N-trichloromethylthiotetrahydrophthalimide,
N-trichloromethylthiophthalimide,
N-dichlorofluoromethylthio-N',N'-dimethyl-N-phenylsulfuric acid diamide,
5-ethoxy-3-trichloromethyl-1,2,3-thiadiazole,
2-thiocyanatomethylthiobenzothiazole,
1,4-dichloro-2,5-dimethoxybenzene,
4-(2-chlorophenylhydrazono)-3-methyl-5-isoxazolone,
2-thiopyridine 1-oxide,
8-hydroxyquinoline and its copper salt,
2,3-dihydro-carboxanilido-6-methyl-1,4-oxathiyne,
2,3-dihydro-carboxanilido-6-methyl-1,4-oxathiyne 4,4-dioxide,
2-methylfuran-3-carboxanilide,
3 2,5-dimethylfuran-3-carboxanilide,
2,4,5-trimethylfuran-3-carboxanilide,
2,5-dimethyl-N-cyclohexylfuran-3-carboxamide,
N-cyclohexyl-N-methoxy-2,5-diethylfuran-3-carboxamide,
2-methylbenzanilide,
2-iodobenzanilide,
N-formyl-N-morpholine-2,2,2-trichloroethylacetal,
piperazine-1,4-diylbis-(1-(2,2,2-trichloroethyl)-formamide),
1-(3,4-dichloroanilino)-1-formylamino-2,2,2-trichloroethane,
2,6-dimethyl-N-tridecylmorpholine and its salts,
2,6-dimethyl-N-cyclododecylmorpholine and its salts,
N-[3-(p-tert.-butylphenyl)-2-methylpropyl]-cis-2,6-dimethylmorpholine,
N-[3-(p-tert.-butylphenyl)-2-methylpropyl]-piperidine,
1-[2-(2,4-dichlorophenyl)-4-ethyl-1-1,3-dioxolan-2-ylethyl]-1H-1,2,4-triazole,
1-[2-(2,4-dichlorophenyl)-4-n-propyl-1,3-dioxolan-2-ylethyl]-1H-1,2,4-triazole,
N-(n-propyl)-N-(2,4,6-trichlorophenoxyethyl)-N'-imidazolyl-urea,
1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-butan-2-one,
1-(4-chlorophenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-butan-2-ol,
1-(4-phenylphenoxy)-3,3-dimethyl-1-(1H-1,2,4-triazol-1-yl)-2-butanol,
α-(2-chlorophenyl)-α-(4-chlorophenyl)-5-pyrimidinemethanol,
5-butyl-(2-dimethylamino-4-hydroxy-6-methylpyrimidine,
bis-(p-chlorophenyl)-3-pyridinemethanol,
1,2-bis-(3-ethoxycarbonyl-2-thioureido)-benzene,
1,2-bis-(3-methoxycarbonyl-2-thioureido)-benzene,
and various fungicides, such as
dodecylguanidine acetate,
3-[3-(3,5-dimethyl-2-oxycyclohexyl)-2-hydroxyethyl]-glutaramide,
hexachlorobenzene,
DL-methyl-N-(2,6-dimethylphenyl)-N-fur-2-yl alenate,
methyl DL-N-(2,6-dimethylphenyl)-N-(2'-methoxyacetyl)-alanate,
N-(2,6-dimethylphenyl)-N-chloroacetyl-DL-2-aminobutyrolactone,
methyl DL-N-(2,6-dimethylphenyl)-N-(phenylacetyl)-alanate,
5-methyl-5-vinyl-3-(3,5-dichlorophenyl)-2,4-dioxo-1,3-oxazolidine,
3-[3,5-dichlorophenyl]-5-methyl-5-methoxymethyl-1,3-oxazolidine-2,4-dione,
3-[3,5-dichlorophenyl]-1-isopropylcarbamylhydantoin,
N-(3,5-dichlorophenyl)-1,2-dimethylcyclopropane-1,2-dicarboximide,
2-cyano-[N-(ethylaminocarbonyl)-2-methoximino]-acetamide,
1-[2-(2,4-dichlorophenyl)-pentyl]-1H-1,2,4-triazole,
2,3-difluoro-α-(1H-1,2,4-triazol-1-ylmethyl)-benzhydryl alcohol,
N-(3-chloro-2,6-dinitro-4-trifluoromethylphenyl)-5-trifluoromethyl-3-chloro-2-aminopyridine, and
1-((bis-(4-fluorophenyl)-methylsilyl)-methyl)-1H-1,2,4-triazole.
For comparison purposes, cis-2-(imidazol-1-yl-methyl)-2-(4-fluorophenyl)-3-(2,6-difluorophenyl)-oxirane (A) disclosed in DE 3,218,130 was used.
Leaves of potted vines of the Muller-Thurgau variety were sprayed with aqueous suspensions containing (dry basis) 80% of active ingredient and 20% of emulsifier. To assess the duration of action, the plants were set up, after the sprayed-on layer had dried, for 8 days in the greenhouse. Then the leaves were infected with a zoospore suspension of Plasmopara viticola. The plants were first placed for 48 hours in a water vapor-saturated chamber at 24° C. and then in a greenhouse for 5 days at from 20° to 30° C. To accelerate and intensify the sporangiophore discharge, the plants were then again placed in the moist chamber for 16 hours. The extent of fungus attack was then assessed on the undersides of the leaves.
The results show that active ingredients 113 and 115, applied as 0.05 wt % spray liquors, had a better fungicidal action (95%) than prior art comparative agent A (60%).
Claims (4)
1. Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes of the general formula I ##STR18## where R1 and R2 are identical or different and each is C1 -C8 -alkyl, C3 -C8 -cycloalkyl, C5 -C8 -cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, each of which is unsubstituted or mono- to trisubstituted by halogen, nitro, phenoxy, amino, alkyl, alkoxy or haloalkyl, each of 1 to 4 carbon atoms,
D is oxygen or a single bond,
E is H, F, Cl or Br,
X, Y and Z are identical or different and each is hydrogen or C1 -C3 -alkyl, X, Y and Z not simultaneously being hydrogen, and acid addition salts and metal complexes thereof tolerated by plants.
2. Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes of the general formula I, where R1 and R2 are phenyl which is unsubstituted or mono- or disubstituted by fluorine, chlorine, bromine or trifluoromethyl.
3. A fungicidal composition comprising a carrier and a fungicidally effective amount of an imidazolylmethyloxirane or an imidazolylpropene of the formula I ##STR19## where R1 and R2 are identical or different and each is C1 -C8 -alkyl, C3 -C8 -cycloalkyl, C5 -C8 -cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, each of which is unsubstituted or mono- to trisubstituted by halogen, nitro, phenoxy, amino, alkyl, alkoxy or haloalkyl, each of 1 to 4 carbon atoms,
D is oxygen or a single bond,
E is H, F, Cl or Br,
X, Y and Z are identical or different and each is hydrogen or C1 -C3 -alkyl, X, Y and Z not simultaneously being hydrogen, and acid addition salt or metal complex thereof tolerated by plants.
4. A process for combating fungi, wherein a fungicidally effective amount of a substituted imidazolylmethyloxirane or of a substituted imidazolylpropene of the formula I ##STR20## where R1 and R2 are identical or different and each is C1 -C8 -alkyl, C3 -C8 -cycloalkyl, C5 -C8 -cycloalkenyl, tetrahydropyranyl, norbornyl, pyridyl, naphthyl, biphenyl or phenyl, each of which is unsubstituted or mono- to trisubstituted by halogen, nitro, phenoxy, amino, alkyl, alkoxy or haloalkyl, each of 1 to 4 carbon atoms,
D is oxygen or a single bond,
E is H, F, Cl or Br,
X, Y and Z are identical or different and each is hydrogen or C1 -C3 -alkyl, X, Y and Z not simultaneously being hydrogen, or an acid addition salt or metal complex thereof tolerated by plants, is allowed to act on the fungi or the materials, areas, plants or seed threatened by fungus attack.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3825586 | 1988-07-28 | ||
| DE3825586A DE3825586A1 (en) | 1988-07-28 | 1988-07-28 | SUBSTITUTED IMIDAZOLYL METHYLOXIRANES AND SUBSTITUTED IMIDAZOLYL PROPENES, THEIR PRODUCTION AND THEIR FUNGICIDES CONTAINING THEM |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/377,000 Division US5028618A (en) | 1988-07-28 | 1989-07-07 | Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes, their preparation and fungicides containing them |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US5098917A true US5098917A (en) | 1992-03-24 |
Family
ID=6359711
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/377,000 Expired - Fee Related US5028618A (en) | 1988-07-28 | 1989-07-07 | Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes, their preparation and fungicides containing them |
| US07/666,189 Expired - Fee Related US5098917A (en) | 1988-07-28 | 1991-03-07 | Substituted imidazolylmethyloxiranes and substituted imidazolypropenes their preparation and fungicides containing them |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US07/377,000 Expired - Fee Related US5028618A (en) | 1988-07-28 | 1989-07-07 | Substituted imidazolylmethyloxiranes and substituted imidazolylpropenes, their preparation and fungicides containing them |
Country Status (11)
| Country | Link |
|---|---|
| US (2) | US5028618A (en) |
| EP (1) | EP0352675A3 (en) |
| JP (1) | JPH0288561A (en) |
| KR (1) | KR910002843A (en) |
| AU (1) | AU610744B2 (en) |
| DD (1) | DD283914A5 (en) |
| DE (1) | DE3825586A1 (en) |
| HU (1) | HU206246B (en) |
| IL (1) | IL90939A0 (en) |
| NZ (1) | NZ230075A (en) |
| ZA (1) | ZA895709B (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7276632B2 (en) | 2003-12-15 | 2007-10-02 | Basf Aktiengesellschaft | Method for the production of 2,3-cis-substituted 2-aryl propenals |
| US20110295019A1 (en) * | 2009-02-05 | 2011-12-01 | Basf Se | Method for Producing Hydroxymethyl Diphenyloxiranes and Corresponding 1-azolylmethyl-1,2-diphenyloxiranes |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3911059A1 (en) * | 1989-04-06 | 1990-10-11 | Basf Ag | 1-ALKOXY-1-AZOLYLMETHYLOXIRANE, METHOD FOR THE PRODUCTION THEREOF AND THEIR USE AS A PLANT PROTECTANT |
| DE3936824A1 (en) * | 1989-11-04 | 1991-05-08 | Basf Ag | N-OXO-AZOLYL METHYLOXIRANES AND FUNGICIDES AND BIOREGULATORS CONTAINING THEM |
| CA2023600A1 (en) * | 1990-08-29 | 1992-02-23 | Wilfred P. Shum | Asymmetric epoxidation using a chiral hydroperoxide |
| DE4217724A1 (en) * | 1992-05-29 | 1993-12-02 | Bayer Ag | 5-haloimidazoles |
| US5484939A (en) * | 1993-03-12 | 1996-01-16 | Lonza Ltd. | 2-substituted 5-chlorimidazoles |
| DE19520097A1 (en) * | 1995-06-01 | 1996-12-05 | Bayer Ag | Triazolylmethyl oxiranes |
| DE19520597A1 (en) * | 1995-06-06 | 1996-12-12 | Bayer Ag | Mercapto-bis-triazoles |
| AU720834B2 (en) * | 1997-03-18 | 2000-06-15 | Ciba Specialty Chemicals Holding Inc. | Photoactivatable nitrogen-containing bases based on alpha-amino alkenes |
| EP0984962B1 (en) * | 1997-05-07 | 2003-04-09 | Basf Aktiengesellschaft | Substituted 4-benzoyl-pyrazoles |
| JP4388997B2 (en) | 2006-09-05 | 2009-12-24 | 協和発酵キリン株式会社 | Imidazole derivatives |
| KR101670035B1 (en) | 2016-07-21 | 2016-10-27 | 장한기술 주식회사 | Heat Storage Module Using Phase Change Material and Manufacturing Method Thereof |
| MX2019003713A (en) * | 2016-09-29 | 2019-06-24 | Bayer Cropscience Ag | 5-substituted imidazolylmethyloxirane derivatives as fungicides. |
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| US4464381A (en) * | 1982-05-14 | 1984-08-07 | Basf Aktiengesellschaft | Fungicides containing azolylmethyloxiranes |
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| CH491132A (en) * | 1965-05-19 | 1970-05-31 | Hoffmann La Roche | Process for the preparation of imidazole derivatives |
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| IL68433A (en) * | 1982-05-14 | 1986-04-29 | Basf Ag | Azolylmethyloxiranes,their manufacture and their use as fungicides and in pharmaceutical compositions |
| DE3327036A1 (en) * | 1983-07-27 | 1985-02-07 | Bayer Ag, 5090 Leverkusen | 3- (1,2,4-TRIAZOL-1-YL) -L-PROPENE |
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| DE3511411A1 (en) * | 1985-03-29 | 1986-10-02 | Basf Ag, 6700 Ludwigshafen | USE OF AZOLYLMETHYLOXIRANES TO COMBAT VIRAL DISEASES |
| DE3809069A1 (en) * | 1988-03-18 | 1989-09-28 | Basf Ag | AZOLYL METHYLALLYL ALCOHOLS AND FUNGICIDES CONTAINING THEM |
| DE3819903A1 (en) * | 1988-06-11 | 1989-12-21 | Basf Ag | 1-HALOGEN-1-AZOLYL-ETHAN DERIVATIVES AND FUNGICIDES CONTAINING THEM |
-
1988
- 1988-07-28 DE DE3825586A patent/DE3825586A1/en not_active Withdrawn
-
1989
- 1989-07-07 US US07/377,000 patent/US5028618A/en not_active Expired - Fee Related
- 1989-07-12 IL IL90939A patent/IL90939A0/en unknown
- 1989-07-22 EP EP89113503A patent/EP0352675A3/en not_active Withdrawn
- 1989-07-25 NZ NZ230075A patent/NZ230075A/en unknown
- 1989-07-26 DD DD89331164A patent/DD283914A5/en unknown
- 1989-07-27 AU AU39004/89A patent/AU610744B2/en not_active Ceased
- 1989-07-27 ZA ZA895709A patent/ZA895709B/en unknown
- 1989-07-27 HU HU893820A patent/HU206246B/en not_active IP Right Cessation
- 1989-07-28 KR KR1019890010707A patent/KR910002843A/en not_active Application Discontinuation
- 1989-07-28 JP JP1194449A patent/JPH0288561A/en active Pending
-
1991
- 1991-03-07 US US07/666,189 patent/US5098917A/en not_active Expired - Fee Related
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| US4464381A (en) * | 1982-05-14 | 1984-08-07 | Basf Aktiengesellschaft | Fungicides containing azolylmethyloxiranes |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7276632B2 (en) | 2003-12-15 | 2007-10-02 | Basf Aktiengesellschaft | Method for the production of 2,3-cis-substituted 2-aryl propenals |
| US20110295019A1 (en) * | 2009-02-05 | 2011-12-01 | Basf Se | Method for Producing Hydroxymethyl Diphenyloxiranes and Corresponding 1-azolylmethyl-1,2-diphenyloxiranes |
| CN102378760A (en) * | 2009-02-05 | 2012-03-14 | 巴斯夫欧洲公司 | Method for producing hydroxymethyl diphenyloxiranes and corresponding 1-azolylmethyl-1,2-diphenyloxiranes |
| US8604071B2 (en) * | 2009-02-05 | 2013-12-10 | Basf Se | Method for producing hydroxymethyl diphenyloxiranes and corresponding 1-azolylmethyl-1,2-diphenyloxiranes |
| CN102378760B (en) * | 2009-02-05 | 2015-06-03 | 巴斯夫欧洲公司 | Method for producing hydroxymethyl diphenyloxiranes and corresponding 1-azolylmethyl-1,2-diphenyloxiranes |
Also Published As
| Publication number | Publication date |
|---|---|
| EP0352675A3 (en) | 1990-04-18 |
| DE3825586A1 (en) | 1990-02-01 |
| IL90939A0 (en) | 1990-02-09 |
| DD283914A5 (en) | 1990-10-31 |
| ZA895709B (en) | 1990-04-25 |
| KR910002843A (en) | 1991-02-26 |
| US5028618A (en) | 1991-07-02 |
| JPH0288561A (en) | 1990-03-28 |
| EP0352675A2 (en) | 1990-01-31 |
| AU610744B2 (en) | 1991-05-23 |
| AU3900489A (en) | 1990-02-01 |
| HUT50586A (en) | 1990-03-28 |
| HU206246B (en) | 1992-10-28 |
| NZ230075A (en) | 1990-12-21 |
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